Clinical Research Coordinator

Description

The Clinical Research Coordinator contributes to the overall

operational management of clinical research / trial / study activities from design,

set up, conduct, through closeout. The position has responsibility for the

implementation of research activities for one or more studies. The incumbent

recognizes and performs necessary tasks to manage projects and prioritizes work

to meet necessary deadlines. The incumbent is responsible for planning and

organizing necessary tasks to ensure adherence to the study protocol and

applicable regulations, such as institutional policy and procedures, FDA Code

of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).

The Clinical Research Coordinator collaborates with the Principal Investigator

(PI), ancillary departments, central research infrastructure teams, sponsors,

institutions, and other entities as needed to support the administration of all

aspects of studies, including, but not limited

to, compliant conduct, financial management, and adequate personnel support.

This is a 24 month, part-time limited position that may convert to career.

Salary Range : $33.63 - $54.11 / Hourly

Qualifications

All Required : Bachelors

Degree or 1-3 years of previous study coordination or clinical research

coordination experience.

Strong

verbal and written communication skills along with strong interpersonal skills

to effectively

establish rapport, and build collaborate relationships.

Strong

organizational capabilities to organize multiple projects and competing

deadlines for efficiency and cost effectiveness.

Analytical

skills sufficient to work and solve address problems and identify solutions

with reasoned judgement.

Ability

to adapt to changing job demands and priorities; work flexible hours to

accommodate research

deadlines.

Ability

to respond to situations in an appropriate and professional manner.

Ability

to concentrate and focus in a work environment that contains distracting

stimuli and competing deadlines.

Ability

to be flexible in handling work delegated by more than one individual.

Typing

and computer skill / ability including word-processing, use of spreadsheets,

email, data entry. Ability to navigate numerous software programs and applications.

Ability

to handle confidential material information with judgement and discretion.

Working

knowledge of the clinical research regulatory framework and institutional

requirements.

Mathematical

skills Sufficient to prepare clinical research budgets, knowledge of math

ability and knowledge

of clinical trials research budgeting process to assist with the preparation of

clinical trial

budgets.

Working

knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical

Practice (GC)

for clinical research.

Be

available to work in more than one environment, travel to meetings, off-site

visits, conferences,

etc.